Evidence map›Paper›PMID 30210615›Full record

ArticleExperimental and therapeutic medicine2018

Efficacy and tolerability of interferon-free regimen for patients with genotype-1 HCV infection.

Kosuke Takeda, Ryuichi Noguchi, Tadashi Namisaki, Kei Moriya, Takemi Akahane, Mitsuteru Kitade, Hideto Kawaratani, Naotaka Shimozato, Kosuke Kaji, Hiroaki Takaya and 17 more

Open access · diamondAbstract read
In one paragraph

Article in Experimental and therapeutic medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.5field-weighted citation impact, top 33% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 7 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

27 authors at 1 institution in 1 country.

Kosuke TakedaThird Department of Internal Medicine, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Ryuichi NoguchiThird Department of Internal Medicine, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Tadashi NamisakiThird Department of Internal Medicine, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Kei MoriyaThird Department of Internal Medicine, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Takemi AkahaneThird Department of Internal Medicine, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Mitsuteru KitadeThird Department of Internal Medicine, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Hideto KawarataniThird Department of Internal Medicine, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Naotaka ShimozatoThird Department of Internal Medicine, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Kosuke KajiThird Department of Internal Medicine, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Hiroaki TakayaThird Department of Internal Medicine, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Yasuhiko SawadaThird Department of Internal Medicine, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Kenichiro SekiThird Department of Internal Medicine, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Yukihisa FujinagaThird Department of Internal Medicine, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Yuki TsujiThird Department of Internal Medicine, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Takuya KuboThird Department of Internal Medicine, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Shinya SatoThird Department of Internal Medicine, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Soichiro SaikawaThird Department of Internal Medicine, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Keisuke NakanishiThird Department of Internal Medicine, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Masanori FurukawaThird Department of Internal Medicine, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Koh KitagawaThird Department of Internal Medicine, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Takahiro OzutsumiThird Department of Internal Medicine, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Daisuke KayaThird Department of Internal Medicine, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Akira MitoroThird Department of Internal Medicine, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Tsuyoshi MashitaniThird Department of Internal Medicine, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Yasushi OkuraDepartment of Endoscopy, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Junichi YamaoDepartment of Endoscopy, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Hitoshi YoshijiThird Department of Internal Medicine, Nara Medical University, Kashihara, Nara 634-8522, Japan.
Nara Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Depression is a major reason for interferon (IFN) therapy cessation. IFN-free direct-acting antiviral (DAA) therapy for depression is not well-documented. Thus, four different IFN-free regimens were assessed in genotype-1 hepatitis C virus (HCV) patients with depression. Overall, 287 HCV genotype-1 patients who received combination therapies with IFN-free DAAs of daclatasvir/asunaprevir (DCV/ASV) (n=84), sofosbuvir/ledipasvir (SOF/LDV) (n=95), ombitasvir/paritaprevir/ritonavir (OBV/PTV/r) (n=74), and elbasvir/grazoprevir (EBR/GZR) (n=34) were included. Treatment-induced depression as a complication of HCV therapy in IFN-free DAA regimens was assessed. The severity of depression was evaluated using the Beck Depression Inventory-II (BDI-II) questionnaire. It was demonstrated that all four DAA regimens achieved similar high efficacy in Japanese patients with HCV genotype-1 infection. Moreover, in seven patients with depression who received the 24-week DCV/ASV treatment regimen, the BDI-II scores significantly increased at week 4 as compared with pretreatment values; furthermore, they decreased below baseline at week 12 despite the rapid decline of serum HCV levels after the initiation of DCV/ASV therapy. The BDI-II scores gradually decreased during therapy in the remaining 77 DCV/ASV-treated patients without depression. The BDI-II scores showed a significant decrease from baseline to the end of treatment with 12-week regimens, including SOF/LDV and EBR/GZR. The 12-week DAA regimen of SOF/LDV and EBR/GZR can be safely used with high efficacy in patients with genotype-1 HCV infection, including those with depression.

Indexed as

BDI-IIdepressiondirect-acting antiviral agentsHCV genotype 1sustained virological response

Identifiers

PMID30210615
PMCPMC6122593
OpenAlexW2883788664

What OpenQuestion holds

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Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.